MeSH Treeview
Query OMIM entry list
607801
LGMD1C
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Gene Frequency
Genetic Processes
Gene Expression
Mutagenesis
Amino Acid Substitution
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 3
Genome
Genome Components
Genes
Genes, Dominant
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Heterozygote
Inheritance Patterns
Genes, Dominant
Phenotype
Sequence Homology
Sequence Homology, Amino Acid
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Musculoskeletal Physiological Processes
Muscle Contraction
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